These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

152 related articles for article (PubMed ID: 19772971)

  • 41. Italian Rett database and biobank.
    Sampieri K; Meloni I; Scala E; Ariani F; Caselli R; Pescucci C; Longo I; Artuso R; Bruttini M; Mencarelli MA; Speciale C; Causarano V; Hayek G; Zappella M; Renieri A; Mari F
    Hum Mutat; 2007 Apr; 28(4):329-35. PubMed ID: 17186495
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Novel mutations in the C-terminal region of the MECP2 gene in Tunisian Rett syndrome patients.
    Fendri-Kriaa N; Rouissi A; Ghorbel R; Mkaouar-Rebai E; Belguith N; Gouider-Khouja N; Fakhfakh F
    J Child Neurol; 2012 May; 27(5):564-8. PubMed ID: 21940684
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Mutation analysis of the HDAC 1, 2, 8 and CDKL5 genes in Rett syndrome patients without mutations in MECP2.
    Huppke P; Ohlenbusch A; Brendel C; Laccone F; Gärtner J
    Am J Med Genet A; 2005 Aug; 137(2):136-8. PubMed ID: 16086395
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Atypical Rett syndrome in a girl with mosaic triple X and MECP2 variant.
    Takahashi S; Takeguchi R; Kuroda M; Tanaka R
    Mol Genet Genomic Med; 2020 Mar; 8(3):e1122. PubMed ID: 31943886
    [TBL] [Abstract][Full Text] [Related]  

  • 45. A catalogue of 863 Rett-syndrome-causing MECP2 mutations and lessons learned from data integration.
    Ehrhart F; Jacobsen A; Rigau M; Bosio M; Kaliyaperumal R; Laros JFJ; Willighagen EL; Valencia A; Roos M; Capella-Gutierrez S; Curfs LMG; Evelo CT
    Sci Data; 2021 Jan; 8(1):10. PubMed ID: 33452270
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Spectrum of MECP2 mutations in Rett syndrome.
    Bienvenu T; Villard L; De Roux N; Bourdon V; Fontes M; Beldjord C; Tardieu M; Jonveaux P; Chelly J;
    Genet Test; 2002; 6(1):1-6. PubMed ID: 12180070
    [TBL] [Abstract][Full Text] [Related]  

  • 47. CX
    Horiuchi M; Smith L; Maezawa I; Jin LW
    Brain Behav Immun; 2017 Feb; 60():106-116. PubMed ID: 26883520
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Drug-resistant epilepsy and epileptic phenotype-EEG association in MECP2 mutated Rett syndrome.
    Buoni S; Zannolli R; Felice CD; Saponari S; Strambi M; Dotti MT; Castrucci E; Corbini L; Orsi A; Hayek J
    Clin Neurophysiol; 2008 Nov; 119(11):2455-8. PubMed ID: 18842453
    [TBL] [Abstract][Full Text] [Related]  

  • 49. [Genotype-phenotype correlations in Rett syndrome: the study of Russian cohort of patients].
    Vorsanova SG; Ulas VIu; Iurov IuB; Giovanucci-Uzielli ML; Demidova IA; Gianti L; Villard L; Iurov IIu; Beresheva AK; Novikov PV
    Zh Nevrol Psikhiatr Im S S Korsakova; 2002; 102(10):23-9. PubMed ID: 12449561
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Survival with Rett syndrome: comparing Rett's original sample with data from the Australian Rett Syndrome Database.
    Freilinger M; Bebbington A; Lanator I; De Klerk N; Dunkler D; Seidl R; Leonard H; Ronen GM
    Dev Med Child Neurol; 2010 Oct; 52(10):962-5. PubMed ID: 20573179
    [TBL] [Abstract][Full Text] [Related]  

  • 51. [Application of long range polymerase chain reaction and DNA direct sequencing in diagnosis of Rett syndrome].
    Li MR; Pan H; Bao XH; Cao GN; Wu XR
    Zhonghua Er Ke Za Zhi; 2007 Aug; 45(8):579-82. PubMed ID: 18021529
    [TBL] [Abstract][Full Text] [Related]  

  • 52. MeCP2_e2 partially compensates for lack of MeCP2_e1: A male case of Rett syndrome.
    Takeguchi R; Takahashi S; Kuroda M; Tanaka R; Suzuki N; Tomonoh Y; Ihara Y; Sugiyama N; Itoh M
    Mol Genet Genomic Med; 2020 Feb; 8(2):e1088. PubMed ID: 31816669
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Analysis of Hungarian patients with Rett syndrome phenotype for MECP2, CDKL5 and FOXG1 gene mutations.
    Hadzsiev K; Polgar N; Bene J; Komlosi K; Karteszi J; Hollody K; Kosztolanyi G; Renieri A; Melegh B
    J Hum Genet; 2011 Mar; 56(3):183-7. PubMed ID: 21160487
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Rett syndrome: methyl-CpG-binding protein 2 mutations and phenotype-genotype correlations.
    Amir RE; Zoghbi HY
    Am J Med Genet; 2000; 97(2):147-52. PubMed ID: 11180222
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Cell cloning-based transcriptome analysis in Rett patients: relevance to the pathogenesis of Rett syndrome of new human MeCP2 target genes.
    Nectoux J; Fichou Y; Rosas-Vargas H; Cagnard N; Bahi-Buisson N; Nusbaum P; Letourneur F; Chelly J; Bienvenu T
    J Cell Mol Med; 2010 Jul; 14(7):1962-74. PubMed ID: 20569274
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Study of MECP2 gene in Rett syndrome variants and autistic girls.
    Zappella M; Meloni I; Longo I; Canitano R; Hayek G; Rosaia L; Mari F; Renieri A
    Am J Med Genet B Neuropsychiatr Genet; 2003 May; 119B(1):102-7. PubMed ID: 12707946
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Inflammatory protein response in CDKL5-Rett syndrome: evidence of a subclinical smouldering inflammation.
    Cortelazzo A; de Felice C; Leoncini S; Signorini C; Guerranti R; Leoncini R; Armini A; Bini L; Ciccoli L; Hayek J
    Inflamm Res; 2017 Mar; 66(3):269-280. PubMed ID: 27900411
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Role of epigenetics in Rett syndrome.
    Kubota T; Miyake K; Hirasawa T
    Epigenomics; 2013; 5(5):583-92. PubMed ID: 24059803
    [TBL] [Abstract][Full Text] [Related]  

  • 59. A rare male patient with classic Rett syndrome caused by MeCP2_e1 mutation.
    Tokaji N; Ito H; Kohmoto T; Naruto T; Takahashi R; Goji A; Mori T; Toda Y; Saito M; Tange S; Masuda K; Kagami S; Imoto I
    Am J Med Genet A; 2018 Mar; 176(3):699-702. PubMed ID: 29341476
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Characterization of large deletions of the MECP2 gene in Rett syndrome patients by gene dosage analysis.
    Vidal S; Pascual-Alonso A; Rabaza-Gairí M; Gerotina E; Brandi N; Pacheco P; Xiol C; Pineda M; ; Armstrong J
    Mol Genet Genomic Med; 2019 Aug; 7(8):e793. PubMed ID: 31206249
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.